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The QC Analytical Senior Analyst is responsible for the timely completion of lot release and testing of pharmaceutical drug substances and drug products under cGMP guidelines. The job involves working independently on advanced assays for multiple products with minimal supervision ...
Novato3 weeks ago
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-12 month contract · -Pay: $ /hr · SUMMARY · The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guideli ...
Novato6 days ago
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The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, · stability,and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines · and procedures. · Performs biochemical ...
Novato3 weeks ago
- Work in company
Senior Director, Analytical Development and Quality Control
Only for registered members
We are seeking a highly experienced analytical and QC leader to join the Technical Operations team as the Head of Analytical Development and Quality Control.The candidate will lead analytical development and quality control for Altos programs. · The successful candidate will have ...
San Francisco, CA1 week ago
- Work in company
Senior Director, Analytical Development and Quality Control
Only for registered members
· Our Mission · Our mission is to restore cell health and resilience through cell rejuvenation to reverse disease, injury, and the disabilities that can occur throughout life. · For more information, see our website at · Our Value · Our Single Altos Value: Everyone Owns Achievi ...
San Francisco Bay Area, CA $283,900 - $384,100 (USD) per year1 week ago
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The Senior Quality Control (QC) Analytical Analyst is responsible for the timely execution of lot release, · stability, and non-routine testing of pharmaceutical drug substances and drug products in compliance with cGMP guidelines.Perform biochemical, physical, and chemical analy ...
Novato3 weeks ago
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This role is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in compliance with cGMP guidelines. · Perform biochemical, physical, and chemical analyses under cGMP with minimal supervision ...
Novato2 weeks ago
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The Senior Analyst, Quality Control Analytical is responsible for the rigorous execution of lot release, · stability and non-routine testing of pharmaceutical drug substances · and products under strict cGMP guidelines. ...
Novato3 weeks ago
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We are seeking a QC Analytical Analyst to support lot release, · stability, · and non-routine testing of pharmaceutical drug substances · and drug products in a cGMP-regulated laboratory environment.This role operates with minimal supervision. · The ideal candidate is comfortable ...
Novato2 weeks ago
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++ The QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. · +Perform biochemical, physical, and chemical analyses of test samples ...
Novato1 week ago
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The BioMarin Summer Internship Program will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, while gaining an insight into the pharmaceutical/biotech industry. · Analytical Services & Process Analytics (AS/PA) supports BioMar ...
Novato $24 - $32 (USD)2 weeks ago
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The BioMarin Summer Internship Program will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin. · Over the course of weeks our interns gain industry experience while working alongside our talented team on meaningful projects. · ...
Novato $24 - $32 (USD) Internship1 month ago
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The QC Analytical Senior Analyst under minimal supervision responsible timely completion lot release stability non routine testing pharmaceutical drug substances drug products adhering cGMP guidelines procedures. · Performs biochemical physical chemical analyses test samples unde ...
Novato3 weeks ago
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The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. · The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide traini ...
Novato2 weeks ago
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About the Role · The Director of Quality provides strategic and operational leadership for network‑wide clinical quality, performance improvement, patient safety, and outcomes optimization across a clinically integrated outpatient network. This role partners closely with affiliat ...
Novato6 days ago
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The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. · The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide traini ...
Novato Full time1 month ago
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The QC Analytical Senior Analyst is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · ...
Novato $31 - $50 (USD)1 month ago
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We are seeking a QC Analytical Analyst to support lot release stability and non-routine testing of pharmaceutical drug substances and drug products in a cGMP regulated laboratory environment. · ...
Novato, CA2 weeks ago
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The intern will improve the quality, · consistency and usability of key VCM documents · and data sources. Required skills include exceptional attention to detail, · proficiency in Microsoft Office Suite and strong organizational capabilities. · Exceptional attention to detail · P ...
Novato1 month ago
- Work in company
Scientist 2, Separations and Biophysical Characterization
Only for registered members
DESCRIPTION · Who We Are · BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. · Since our founding in 1997, we have applied our scientific expertise in und ...
Novato Full time2 days ago
Senior Analyst, Quality Control Analytical - Novato - Planet Pharma
Description
-12 month contract
-Pay: $ /hr
Make sure to apply quickly in order to maximise your chances of being considered for an interview Read the complete job description below.
SUMMARY
The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.
The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. Work assignments will encompass performing and documenting activities and requires the ability to recognize deviations from approved procedures. Good record keeping, organizational, and written and verbal communication skills are essential.
The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide training and educational development of other staff.
RESPONSIBILITIES
• Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines
• Works independently on assays they have mastered
• Develops and maintains proficiency in a broad range of test methods
• Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations
• Evaluates data against defined criteria/specifications
• Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices
• Identifies key issues in complex situations, analyzes problems, and makes sound decisions
• Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned
• Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise
• Holds self and others accountable for adherence to department and company policies and practices
• Maintains a safety and quality focused culture
EXPERIENCE
Required Skills:
• 3+ years of experience in a cGMP/GLP laboratory
• 2+ years hands-on experience in separation sciences (HPLC, UPLC, xhmxlyz CE)
• Ability to follow written instructions and to perform tasks with direct or minimal supervision
• Strong leadership skills demonstrated through past work history
• Use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel
• Good written and verbal communication skills
• Attention to detail and strong documentation skills
• Ability to contribute effectively in team environments and independently
Desired Skills:
• 3-5 years of Quality Control laboratory experience
• 3-5 years of hands-on experience in separation sciences (HPLC, UPLC, CE)
EDUCATION
• B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry).
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